Name: rs10004411
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10004411

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:1360518 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.234554 (62084/264690, TOPMED)
G=0.226839 (31772/140064, GnomAD)
G=0.28340 (22300/78686, PAGE_STUDY) (+ 17 more)
G=0.22614 (6389/28252, 14KJPN)
G=0.18026 (3492/19372, ALFA)
G=0.22667 (3799/16760, 8.3KJPN)
G=0.2448 (1568/6404, 1000G_30x)
G=0.2382 (1193/5008, 1000G)
G=0.1018 (456/4480, Estonian)
G=0.1419 (547/3854, ALSPAC)
G=0.1448 (537/3708, TWINSUK)
G=0.1997 (585/2930, KOREAN)
G=0.2211 (405/1832, Korea1K)
G=0.128 (128/998, GoNL)
G=0.137 (82/600, NorthernSweden)
G=0.208 (45/216, Qatari)
G=0.150 (32/214, Vietnamese)
T=0.438 (78/178, SGDP_PRJ)
G=0.17 (7/40, GENOME_DK)
T=0.38 (6/16, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UVSSA : Non Coding Transcript Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	19372	T=0.81974	G=0.18026
European	Sub	14364	T=0.87190	G=0.12810
African	Sub	2978	T=0.5772	G=0.4228
African Others	Sub	114	T=0.596	G=0.404
African American	Sub	2864	T=0.5765	G=0.4235
Asian	Sub	150	T=0.747	G=0.253
East Asian	Sub	122	T=0.779	G=0.221
Other Asian	Sub	28	T=0.61	G=0.39
Latin American 1	Sub	154	T=0.766	G=0.234
Latin American 2	Sub	616	T=0.833	G=0.167
South Asian	Sub	104	T=0.817	G=0.183
Other	Sub	1006	T=0.8042	G=0.1958

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.765446	G=0.234554
gnomAD - Genomes	Global	Study-wide	140064	T=0.773161	G=0.226839
gnomAD - Genomes	European	Sub	75874	T=0.86505	G=0.13495
gnomAD - Genomes	African	Sub	41938	T=0.57540	G=0.42460
gnomAD - Genomes	American	Sub	13654	T=0.83939	G=0.16061
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.8914	G=0.1086
gnomAD - Genomes	East Asian	Sub	3124	T=0.7705	G=0.2295
gnomAD - Genomes	Other	Sub	2150	T=0.7884	G=0.2116
The PAGE Study	Global	Study-wide	78686	T=0.71660	G=0.28340
The PAGE Study	AfricanAmerican	Sub	32506	T=0.57989	G=0.42011
The PAGE Study	Mexican	Sub	10810	T=0.86485	G=0.13515
The PAGE Study	Asian	Sub	8316	T=0.7643	G=0.2357
The PAGE Study	PuertoRican	Sub	7914	T=0.7914	G=0.2086
The PAGE Study	NativeHawaiian	Sub	4534	T=0.8586	G=0.1414
The PAGE Study	Cuban	Sub	4230	T=0.8170	G=0.1830
The PAGE Study	Dominican	Sub	3828	T=0.7325	G=0.2675
The PAGE Study	CentralAmerican	Sub	2450	T=0.8249	G=0.1751
The PAGE Study	SouthAmerican	Sub	1982	T=0.8219	G=0.1781
The PAGE Study	NativeAmerican	Sub	1260	T=0.8246	G=0.1754
The PAGE Study	SouthAsian	Sub	856	T=0.848	G=0.152
14KJPN	JAPANESE	Study-wide	28252	T=0.77386	G=0.22614
Allele Frequency Aggregator	Total	Global	19372	T=0.81974	G=0.18026
Allele Frequency Aggregator	European	Sub	14364	T=0.87190	G=0.12810
Allele Frequency Aggregator	African	Sub	2978	T=0.5772	G=0.4228
Allele Frequency Aggregator	Other	Sub	1006	T=0.8042	G=0.1958
Allele Frequency Aggregator	Latin American 2	Sub	616	T=0.833	G=0.167
Allele Frequency Aggregator	Latin American 1	Sub	154	T=0.766	G=0.234
Allele Frequency Aggregator	Asian	Sub	150	T=0.747	G=0.253
Allele Frequency Aggregator	South Asian	Sub	104	T=0.817	G=0.183
8.3KJPN	JAPANESE	Study-wide	16760	T=0.77333	G=0.22667
1000Genomes_30x	Global	Study-wide	6404	T=0.7552	G=0.2448
1000Genomes_30x	African	Sub	1786	T=0.5482	G=0.4518
1000Genomes_30x	Europe	Sub	1266	T=0.8491	G=0.1509
1000Genomes_30x	South Asian	Sub	1202	T=0.8536	G=0.1464
1000Genomes_30x	East Asian	Sub	1170	T=0.7821	G=0.2179
1000Genomes_30x	American	Sub	980	T=0.858	G=0.142
1000Genomes	Global	Study-wide	5008	T=0.7618	G=0.2382
1000Genomes	African	Sub	1322	T=0.5590	G=0.4410
1000Genomes	East Asian	Sub	1008	T=0.7857	G=0.2143
1000Genomes	Europe	Sub	1006	T=0.8529	G=0.1471
1000Genomes	South Asian	Sub	978	T=0.849	G=0.151
1000Genomes	American	Sub	694	T=0.859	G=0.141
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8982	G=0.1018
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8581	G=0.1419
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8552	G=0.1448
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8003	G=0.1997
Korean Genome Project	KOREAN	Study-wide	1832	T=0.7789	G=0.2211
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.872	G=0.128
Northern Sweden	ACPOP	Study-wide	600	T=0.863	G=0.137
Qatari	Global	Study-wide	216	T=0.792	G=0.208
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.850	G=0.150
SGDP_PRJ	Global	Study-wide	178	T=0.438	G=0.562
The Danish reference pan genome	Danish	Study-wide	40	T=0.82	G=0.17
Siberian	Global	Study-wide	16	T=0.38	G=0.62

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 4	NC_000004.12:g.1360518T>G
GRCh37.p13 chr 4	NC_000004.11:g.1354306T>G
UVSSA RefSeqGene	NG_032753.1:g.18203T>G

Gene: UVSSA, UV stimulated scaffold protein A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UVSSA transcript variant 2	NM_001317934.2:c.1176+527… NM_001317934.2:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant 3	NM_001317935.2:c.1176+527… NM_001317935.2:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant 1	NM_020894.4:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X6	XM_017008490.1:c.1176+527… XM_017008490.1:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X5	XM_017008492.3:c.1176+527… XM_017008492.3:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X8	XM_017008493.3:c.1176+527… XM_017008493.3:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X7	XM_017008494.3:c.1176+527… XM_017008494.3:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X9	XM_017008495.2:c.888+5273… XM_017008495.2:c.888+5273T>G	N/A	Intron Variant
UVSSA transcript variant X16	XM_017008498.3:c.1176+527… XM_017008498.3:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X20	XM_024454162.2:c.-172+527… XM_024454162.2:c.-172+5273T>G	N/A	Intron Variant
UVSSA transcript variant X3	XM_047416025.1:c.1176+527… XM_047416025.1:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X4	XM_047416026.1:c.1176+527… XM_047416026.1:c.1176+5273T>G	N/A	Intron Variant
UVSSA transcript variant X14	XM_047416027.1:c.834+5273… XM_047416027.1:c.834+5273T>G	N/A	Intron Variant
UVSSA transcript variant X18	XM_047416028.1:c.1177-399… XM_047416028.1:c.1177-3990T>G	N/A	Intron Variant
UVSSA transcript variant X10	XM_017008496.2:c.*3979=	N/A	3 Prime UTR Variant
UVSSA transcript variant X19	XM_017008500.1:c.	N/A	Genic Upstream Transcript Variant
UVSSA transcript variant X15	XM_017008497.3:c.	N/A	Genic Downstream Transcript Variant
UVSSA transcript variant X17	XM_017008499.2:c.	N/A	Genic Downstream Transcript Variant
UVSSA transcript variant X11	XR_001741303.2:n.5309T>G	N/A	Non Coding Transcript Variant
UVSSA transcript variant X12	XR_001741302.2:n.5294T>G	N/A	Non Coding Transcript Variant
UVSSA transcript variant X13	XR_001741304.2:n.5596T>G	N/A	Non Coding Transcript Variant
UVSSA transcript variant X1	XR_007057948.1:n.	N/A	Intron Variant
UVSSA transcript variant X2	XR_007057949.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	T=	G
GRCh38.p14 chr 4	NC_000004.12:g.1360518=	NC_000004.12:g.1360518T>G
GRCh37.p13 chr 4	NC_000004.11:g.1354306=	NC_000004.11:g.1354306T>G
UVSSA RefSeqGene	NG_032753.1:g.18203=	NG_032753.1:g.18203T>G
UVSSA transcript variant X10	XM_017008496.2:c.*3979=	XM_017008496.2:c.*3979T>G
UVSSA transcript variant X11	XM_017008496.1:c.*3979=	XM_017008496.1:c.*3979T>G
UVSSA transcript variant X13	XR_001741304.2:n.5596=	XR_001741304.2:n.5596T>G
UVSSA transcript variant X14	XR_001741304.1:n.6104=	XR_001741304.1:n.6104T>G
UVSSA transcript variant X11	XR_001741303.2:n.5309=	XR_001741303.2:n.5309T>G
UVSSA transcript variant X13	XR_001741303.1:n.5817=	XR_001741303.1:n.5817T>G
UVSSA transcript variant X12	XR_001741302.2:n.5294=	XR_001741302.2:n.5294T>G
UVSSA transcript variant X12	XR_001741302.1:n.5802=	XR_001741302.1:n.5802T>G
UVSSA transcript variant 2	NM_001317934.2:c.1176+5273=	NM_001317934.2:c.1176+5273T>G
UVSSA transcript variant 3	NM_001317935.2:c.1176+5273=	NM_001317935.2:c.1176+5273T>G
UVSSA transcript	NM_020894.2:c.1176+5273=	NM_020894.2:c.1176+5273T>G
UVSSA transcript variant 1	NM_020894.4:c.1176+5273=	NM_020894.4:c.1176+5273T>G
UVSSA transcript variant X1	XM_005272290.1:c.1176+5273=	XM_005272290.1:c.1176+5273T>G
UVSSA transcript variant X2	XM_005272291.1:c.1176+5273=	XM_005272291.1:c.1176+5273T>G
UVSSA transcript variant X3	XM_005272292.1:c.1176+5273=	XM_005272292.1:c.1176+5273T>G
UVSSA transcript variant X6	XM_017008490.1:c.1176+5273=	XM_017008490.1:c.1176+5273T>G
UVSSA transcript variant X5	XM_017008492.3:c.1176+5273=	XM_017008492.3:c.1176+5273T>G
UVSSA transcript variant X8	XM_017008493.3:c.1176+5273=	XM_017008493.3:c.1176+5273T>G
UVSSA transcript variant X7	XM_017008494.3:c.1176+5273=	XM_017008494.3:c.1176+5273T>G
UVSSA transcript variant X9	XM_017008495.2:c.888+5273=	XM_017008495.2:c.888+5273T>G
UVSSA transcript variant X16	XM_017008498.3:c.1176+5273=	XM_017008498.3:c.1176+5273T>G
UVSSA transcript variant X20	XM_024454162.2:c.-172+5273=	XM_024454162.2:c.-172+5273T>G
UVSSA transcript variant X3	XM_047416025.1:c.1176+5273=	XM_047416025.1:c.1176+5273T>G
UVSSA transcript variant X4	XM_047416026.1:c.1176+5273=	XM_047416026.1:c.1176+5273T>G
UVSSA transcript variant X14	XM_047416027.1:c.834+5273=	XM_047416027.1:c.834+5273T>G
UVSSA transcript variant X18	XM_047416028.1:c.1177-3990=	XM_047416028.1:c.1177-3990T>G

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

69 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13850256	Dec 05, 2003 (119)
2	BCMHGSC_JDW	ss92438535	Mar 24, 2008 (129)
3	BGI	ss104032161	Dec 01, 2009 (131)
4	ILLUMINA-UK	ss116836712	Feb 14, 2009 (130)
5	ENSEMBL	ss139393719	Dec 01, 2009 (131)
6	GMI	ss156743751	Dec 01, 2009 (131)
7	COMPLETE_GENOMICS	ss161888249	Jul 04, 2010 (132)
8	COMPLETE_GENOMICS	ss162993836	Jul 04, 2010 (132)
9	1000GENOMES	ss211343114	Jul 14, 2010 (132)
10	1000GENOMES	ss220692350	Jul 14, 2010 (132)
11	1000GENOMES	ss232224359	Jul 14, 2010 (132)
12	1000GENOMES	ss239553620	Jul 15, 2010 (132)
13	GMI	ss277538653	May 04, 2012 (137)
14	PJP	ss293053505	May 09, 2011 (134)
15	ILLUMINA	ss536528498	Sep 08, 2015 (146)
16	TISHKOFF	ss557252450	Apr 25, 2013 (138)
17	SSMP	ss651005854	Apr 25, 2013 (138)
18	EVA-GONL	ss979670767	Aug 21, 2014 (142)
19	JMKIDD_LAB	ss1071213709	Aug 21, 2014 (142)
20	1000GENOMES	ss1308079164	Aug 21, 2014 (142)
21	EVA_GENOME_DK	ss1580379497	Apr 01, 2015 (144)
22	EVA_DECODE	ss1589167122	Apr 01, 2015 (144)
23	EVA_UK10K_ALSPAC	ss1609231819	Apr 01, 2015 (144)
24	EVA_UK10K_TWINSUK	ss1652225852	Apr 01, 2015 (144)
25	HAMMER_LAB	ss1800790473	Sep 08, 2015 (146)
26	WEILL_CORNELL_DGM	ss1922901466	Feb 12, 2016 (147)
27	ILLUMINA	ss1958650187	Feb 12, 2016 (147)
28	JJLAB	ss2022024521	Sep 14, 2016 (149)
29	USC_VALOUEV	ss2150130489	Dec 20, 2016 (150)
30	HUMAN_LONGEVITY	ss2259804500	Dec 20, 2016 (150)
31	SYSTEMSBIOZJU	ss2625513373	Nov 08, 2017 (151)
32	GRF	ss2705564914	Nov 08, 2017 (151)
33	GNOMAD	ss2804661254	Nov 08, 2017 (151)
34	SWEGEN	ss2993988815	Nov 08, 2017 (151)
35	ILLUMINA	ss3022336556	Nov 08, 2017 (151)
36	BIOINF_KMB_FNS_UNIBA	ss3024781866	Nov 08, 2017 (151)
37	CSHL	ss3345497368	Nov 08, 2017 (151)
38	ILLUMINA	ss3625836108	Oct 12, 2018 (152)
39	ILLUMINA	ss3628883403	Oct 12, 2018 (152)
40	ILLUMINA	ss3652819026	Oct 12, 2018 (152)
41	EGCUT_WGS	ss3661927066	Jul 13, 2019 (153)
42	EVA_DECODE	ss3711231715	Jul 13, 2019 (153)
43	ILLUMINA	ss3726101771	Jul 13, 2019 (153)
44	ACPOP	ss3730776188	Jul 13, 2019 (153)
45	EVA	ss3761281990	Jul 13, 2019 (153)
46	PAGE_CC	ss3771099229	Jul 13, 2019 (153)
47	KHV_HUMAN_GENOMES	ss3804421631	Jul 13, 2019 (153)
48	EVA	ss3828324957	Apr 25, 2020 (154)
49	SGDP_PRJ	ss3858018062	Apr 25, 2020 (154)
50	KRGDB	ss3904144684	Apr 25, 2020 (154)
51	KOGIC	ss3953348239	Apr 25, 2020 (154)
52	TOPMED	ss4600095034	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5163806862	Apr 26, 2021 (155)
54	EVA	ss5237341806	Apr 26, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5257733822	Oct 13, 2022 (156)
56	EVA	ss5346357252	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5456688983	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5538028148	Oct 13, 2022 (156)
59	SANFORD_IMAGENETICS	ss5624544964	Oct 13, 2022 (156)
60	SANFORD_IMAGENETICS	ss5634168951	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5697338356	Oct 13, 2022 (156)
62	YY_MCH	ss5804675503	Oct 13, 2022 (156)
63	EVA	ss5843425412	Oct 13, 2022 (156)
64	EVA	ss5847235522	Oct 13, 2022 (156)
65	EVA	ss5847998351	Oct 13, 2022 (156)
66	EVA	ss5854045482	Oct 13, 2022 (156)
67	EVA	ss5861806650	Oct 13, 2022 (156)
68	EVA	ss5962544448	Oct 13, 2022 (156)
69	EVA	ss5979687632	Oct 13, 2022 (156)
70	1000Genomes	NC_000004.11 - 1354306	Oct 12, 2018 (152)
71	1000Genomes_30x	NC_000004.12 - 1360518	Oct 13, 2022 (156)
72	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 1354306	Oct 12, 2018 (152)
73	Genetic variation in the Estonian population	NC_000004.11 - 1354306	Oct 12, 2018 (152)
74	The Danish reference pan genome	NC_000004.11 - 1354306	Apr 25, 2020 (154)
75	gnomAD - Genomes	NC_000004.12 - 1360518	Apr 26, 2021 (155)
76	Genome of the Netherlands Release 5	NC_000004.11 - 1354306	Apr 25, 2020 (154)
77	KOREAN population from KRGDB	NC_000004.11 - 1354306	Apr 25, 2020 (154)
78	Korean Genome Project	NC_000004.12 - 1360518	Apr 25, 2020 (154)
79	Northern Sweden	NC_000004.11 - 1354306	Jul 13, 2019 (153)
80	The PAGE Study	NC_000004.12 - 1360518	Jul 13, 2019 (153)
81	Qatari	NC_000004.11 - 1354306	Apr 25, 2020 (154)
82	SGDP_PRJ	NC_000004.11 - 1354306	Apr 25, 2020 (154)
83	Siberian	NC_000004.11 - 1354306	Apr 25, 2020 (154)
84	8.3KJPN	NC_000004.11 - 1354306	Apr 26, 2021 (155)
85	14KJPN	NC_000004.12 - 1360518	Oct 13, 2022 (156)
86	TopMed	NC_000004.12 - 1360518	Apr 26, 2021 (155)
87	UK 10K study - Twins	NC_000004.11 - 1354306	Oct 12, 2018 (152)
88	A Vietnamese Genetic Variation Database	NC_000004.11 - 1354306	Jul 13, 2019 (153)
89	ALFA	NC_000004.12 - 1360518	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss92438535, ss116836712, ss161888249, ss162993836, ss211343114, ss277538653, ss293053505, ss1589167122	NC_000004.10:1344305:T:G	NC_000004.12:1360517:T:G	(self)
19416801, 10823473, 7665314, 6544436, 4757314, 11322078, 4061053, 4943396, 10035042, 2646843, 21776169, 10823473, 2366578, ss220692350, ss232224359, ss239553620, ss536528498, ss557252450, ss651005854, ss979670767, ss1071213709, ss1308079164, ss1580379497, ss1609231819, ss1652225852, ss1800790473, ss1922901466, ss1958650187, ss2022024521, ss2150130489, ss2625513373, ss2705564914, ss2804661254, ss2993988815, ss3022336556, ss3345497368, ss3625836108, ss3628883403, ss3652819026, ss3661927066, ss3730776188, ss3761281990, ss3828324957, ss3858018062, ss3904144684, ss5163806862, ss5237341806, ss5346357252, ss5624544964, ss5634168951, ss5843425412, ss5847235522, ss5847998351, ss5962544448, ss5979687632	NC_000004.11:1354305:T:G	NC_000004.12:1360517:T:G	(self)
25554083, 137840247, 9726240, 320698, 31175460, 437472590, 13051726554, ss2259804500, ss3024781866, ss3711231715, ss3726101771, ss3771099229, ss3804421631, ss3953348239, ss4600095034, ss5257733822, ss5456688983, ss5538028148, ss5697338356, ss5804675503, ss5854045482, ss5861806650	NC_000004.12:1360517:T:G	NC_000004.12:1360517:T:G	(self)
ss13850256	NT_037622.3:1344135:T:G	NC_000004.12:1360517:T:G	(self)
ss104032161, ss139393719, ss156743751	NT_037622.5:1344305:T:G	NC_000004.12:1360517:T:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10004411

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10004411